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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925050Generated: October 30, 2026

Chlorodiphenylphosphine → HCID 178483811, compound

https://huagongshe.com/reaction/925050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodiphenylphosphineHCID 66180—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178483800HCID 178483800—
ProductHCID 178483811HCID 178483811—

Reaction Steps

Procedure as described for NP Amidine I using the following amounts and modifications: 0.956 g of N1-(2-(dimethylamino)ethyl)benzamidine (Amidine XII, 5.0 mmol), 2.50 mL of 2.0 M butyllithium (5.0 mmol), 0.93 mL chlorodiphenylphosphine (5.0 mmol). After filtration to remove lithium chloride and removal of solvent, the oily product was treated with 20 mL of pentane. After 1 hour stiffing at room temperature, a white solid formed. The solution was concentrated to approximately 10 mL and filtered while cold, yielding 0.891 g (47%) after drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09283555B2
Source datasetuspto-grants-2016_03
ORD IDord-504133c5c84544a18118f8ab16fdae79
Source noteuspto-grants-2016_03